Term Name: cranioectodermal dysplasia 2
Synonyms:
Definition: A cranioectodermal dysplasia that has_material_basis_in compound heterozygous mutation in the WDR35 gene on chromosome 2p24.
Ontology: Human Disease [DOID:0080804]   (DOID:0080804)

Relationships
is a type of: cranioectodermal dysplasia